Examples
- rs6311 and rs6313 are SNPs in the HTR2A gene on human chromosome 13.
- A SNP in the F5 gene causes a hypercoagulability disorder with the variant Factor V Leiden.
- rs3091244 is an example of a triallelic SNP in the CRP gene on human chromosome 1.
- TAS2R38 codes for PTC tasting ability, and contains 6 annotated SNPs.
- rs148649884 and rs138055828 in the FCN1 gene encoding M-ficolin crippled the ligand-binding capability of the recombinant M-ficolin.
Read more about this topic: Single Nucleotide Polymorphism
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